Colon Cancer: Gene >> CA5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309893
Start	87888266:87888266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309893
Start	87926766:87926766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570806518
CDS Mutation	c.322G>A
AA Mutation	p.Asp108Asn(p.D108N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309893
Start	87891881:87891881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373280084
CDS Mutation	c.692C>T
AA Mutation	p.Ala231Val(p.A231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309893
Start	87888165:87888165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150891997
CDS Mutation	c.882G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309893
Start	87902467:87902467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769040032
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309893
Start	87891853:87891853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547918689
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309893
Start	87936439:87936439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309893
Start	87902429:87902429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.551delT
AA Mutation	p.Leu184Ter(p.L184*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CA5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309893
Start	87902498:87902498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482C>A
AA Mutation	p.Ser161Tyr(p.S161Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309893
Start	87902491:87902491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489A>C
AA Mutation	p.Lys163Asn(p.K163N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript